Erskine Academy girls basketball team holds fundraiser for Multiple Sclerosis

Participants in the Erskine Academy girls basketball team fundraiser for Multiple Sclerosis, held at the school on January 26. Over $500 was raised for those stricken with MS, who need help with medical bills. (photo courtesy of Jane Golden)

Cassidy Roderick, left, with Erskine girls basketball coach Bob Witts. (photo courtesy of Jane Golden)

The Erskine Academy girls’ basketball team hosted a charity basketball clinic on January 26 with proceeds going to the Maine chapter of the National Multiple Sclerosis Society. Thirty-five athletes between the ages of 8 and 12 came to the two-hour clinic to not only learn skills, but to also help raise funds for this worthy cause. Coach Bob Witts and several members of the girls’ basketball team worked with the clinic participants to run them through fun drills, teach them skills, and to play a few games.

Over $550 was raised at this event, which will go towards getting wheelchairs and walkers for people as well as helping pay medical bills for those that cannot afford it in Maine with multiple sclerosis (MS).

One of the Erskine basketball players, Mackenzie Roderick, has been personally affected by MS, as her sister, Cassidy, was diagnosed with the disease a year and a half ago, making this cause very special to her and her teammates. Cassidy joined the participants at the clinic, speaking to the kids and parents about how her wheelchair helps her, especially when she needs to walk a great distance or for a long amount of time.

This was a great way to inform the community about MS and its effects on the lives of those who have it. Congratulations to the Erskine Academy girls’ basketball team for holding such an important fundraiser, and thank you to the community for supporting this cause!

Submitted by Jane Golden, VP of HR, JMG Central Office, 65 Stone Street, Augusta, ME 04330.

 
 

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1 reply
  1. Stella Lynch
    Stella Lynch says:

    I was living with MS for years before being officially diagnosed in 2021. I got annual MRIs, and I did not take any meds due to side effects. I had one flare up in 2021. My legs decided to a break, and I was numb from the waist down. I decided to try MS-4 from Uine Health Centre. The numbness and Muscle spasms went away after a couple of weeks, but it took almost 3 months to walk properly without a cane. In June, it will be four years without incident, and I am extremely happy that I made the decision to not take any meds and went for the MS-4 formula even though my neurologist got upset and one told me to quit my job because I will be disabled. Well, I am not disabled, I still refuse to take those meds, and I am doing just fine. Believe in yourself and go with your instincts. Doctors don’t know it all. I’m surprised a lot of people with MS haven’t heard of the MS-4 protocol, I got the treatment from uinehealth centre . c om I am absolutely confident that this protocol offers a viable solution. I hope you find it helpful

    Reply

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